Engineer, Quality in Minneapolis, MN at Volt

Date Posted: 11/23/2019

Job Snapshot

Job Description

Quality Engineer-Bi-lingual preferred

Plymouth-1 year contract


This is an exciting opportunity for a Quality Engineer that would be open to traveling to Costa Rica about 20% of time.  You would be doing validations on product development, writing quality plans and reports, based in Plymouth overseeing Costa Rica.


The purpose of this position is to initiate medical device quality assurance activities. These activities must be in accordance with FDA Quality System Regulation, ISO 13485 and other international standards.

Essential Duties and Responsibilities:

  • Provide in-process QA support to include inspection and document review.
  • Complete final acceptance activities.
  • Manage the sterilization process, including validations and product sterile loads.
  • Track nonconforming material and lead Material Review Board (MRB) efforts.
  • Manage corrective action and quality improvement activities. Manage aspects of internal quality system relating to receiving inspection, calibration, MRB, etc.
  • Assist in the performance of quality system internal auditing. Support quarterly management review meetings. 

Volt is an Equal Opportunity Employer